1266102-44-6

Basic information

• Product Name: C₄₁H₅₄O₆
• Synonyms: C₄₁H₅₄O₆
• CAS NO: 1266102-44-6
• Molecular Weight: 642.876
• Mol File: 1266102-44-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₄₁H₅₄O₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₄₁H₅₄O₆(1266102-44-6)
• EPA Substance Registry System: C₄₁H₅₄O₆(1266102-44-6)

Safety Data

• Hazardous Substances Data: 1266102-44-6(Hazardous Substances Data)

Upstream product

• 1246949-44-9 3-OTBS-11-ketotigogenin 
• 1246949-45-0 C₃₄H₄₆O₅ 
• 107297-16-5 C₂₇H₄₄O₄ 
• 1246949-40-5 C₃₉H₇₀O₄Si₂ 
• 1246949-41-6 C₃₃H₅₆O₅Si 
• 156590-69-1 (3β,5α,12β,25R)-3-(t-butyldimethylsilyloxy)spirostan-12-ol-11-one 
• 1246949-43-8 C₃₅H₅₈O₆Si 
• 1266102-43-5 C₄₁H₅₂O₆ 
• 467-55-0 hecogenin 
• 4802-74-8 11-ketotigogenin 
• 915-35-5 hecogenin acetate 

Downstream Products

• 1266102-67-3 C₄₁H₅₃IO₅ 
• 1266102-45-7 C₄₁H₅₂O₅ 
• 1266102-46-8 C₄₁H₅₄O₆ 
• 1266102-47-9 C₄₁H₅₂O₆ 
• 1266102-48-0 C₄₁H₅₂O₆ 

Relevant articles and documents

Synthesis of the antiproliferative agent hippuristanol and its analogues via Suárez cyclizations and Hg(II)-catalyzed spiroketalizations

A full account of the synthesis of hippuristanol and its analogues is described. Hecogenin acetate was identified as a suitable and economical starting material for this work, and substrate-controlled stereoselection was obtained throughout the construction of the key spiroketal unit. Suárez cyclization was first used, but Hg(II)-catalyzed spiroketalization of the 3-alkyne-1,7-diol motif was finally identified as the most convenient strategy.(Figure Presented)